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Thomas Quertermous

Showing results (201-210 of 279) with videos related to

Pageof 28
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Circulation|September 10, 2003
Novel role for the potent endogenous inotrope apelin in human cardiac dysfunctionMary M Chen, Euan A Ashley, David X F Deng, et al.
Human Genetics|March 29, 2008
Common polymorphisms of ALOX5 and ALOX5AP and risk of coronary artery diseaseThemistocles L Assimes, Joshua W Knowles, James R Priest, et al.
Science Translational Medicine|September 15, 2017
Endothelial APLNR regulates tissue fatty acid uptake and is essential for apelin's glucose-lowering effectsCheol Hwangbo, Jingxia Wu, Irinna Papangeli, et al.
Nature|August 15, 2014
A long noncoding RNA protects the heart from pathological hypertrophyPei Han, Wei Li, Chiou-Hong Lin, et al.
Plos Genetics|May 29, 2015
Coronary Artery Disease Associated Transcription Factor TCF21 Regulates Smooth Muscle Precursor Cells That Contribute to the Fibrous CapSylvia T Nurnberg, Karen Cheng, Azad Raiesdana, et al.
Physiological Genomics|June 9, 2005
Pathway analysis of coronary atherosclerosisJennifer Y King, Rossella Ferrara, Raymond Tabibiazar, et al.
Nature Communications|July 9, 2016
Integrative functional genomics identifies regulatory mechanisms at coronary artery disease lociClint L Miller, Milos Pjanic, Ting Wang, et al.
Plos One|March 17, 2016
Genetics of Coronary Artery Disease in Taiwan: A Cardiometabochip Study by the Taichi ConsortiumThemistocles L Assimes, I-T Lee, Jyh-Ming Juang, et al.
Nature Medicine|July 31, 2019
Atheroprotective roles of smooth muscle cell phenotypic modulation and the TCF21 disease gene as revealed by single-cell analysisRobert C Wirka, Dhananjay Wagh, David T Paik, et al.
Plos Genetics|January 10, 2020
Genomic profiling of human vascular cells identifies TWIST1 as a causal gene for common vascular diseasesSylvia T Nurnberg, Marie A Guerraty, Robert C Wirka, et al.
Pageof 28

Showing results (201-210 of 279) with videos related to

Sort By:
Pageof 28
Circulation|September 10, 2003
Novel role for the potent endogenous inotrope apelin in human cardiac dysfunctionMary M Chen, Euan A Ashley, David X F Deng, et al.
Human Genetics|March 29, 2008
Common polymorphisms of ALOX5 and ALOX5AP and risk of coronary artery diseaseThemistocles L Assimes, Joshua W Knowles, James R Priest, et al.
Science Translational Medicine|September 15, 2017
Endothelial APLNR regulates tissue fatty acid uptake and is essential for apelin's glucose-lowering effectsCheol Hwangbo, Jingxia Wu, Irinna Papangeli, et al.
Nature|August 15, 2014
A long noncoding RNA protects the heart from pathological hypertrophyPei Han, Wei Li, Chiou-Hong Lin, et al.
Plos Genetics|May 29, 2015
Coronary Artery Disease Associated Transcription Factor TCF21 Regulates Smooth Muscle Precursor Cells That Contribute to the Fibrous CapSylvia T Nurnberg, Karen Cheng, Azad Raiesdana, et al.
Physiological Genomics|June 9, 2005
Pathway analysis of coronary atherosclerosisJennifer Y King, Rossella Ferrara, Raymond Tabibiazar, et al.
Nature Communications|July 9, 2016
Integrative functional genomics identifies regulatory mechanisms at coronary artery disease lociClint L Miller, Milos Pjanic, Ting Wang, et al.
Plos One|March 17, 2016
Genetics of Coronary Artery Disease in Taiwan: A Cardiometabochip Study by the Taichi ConsortiumThemistocles L Assimes, I-T Lee, Jyh-Ming Juang, et al.
Nature Medicine|July 31, 2019
Atheroprotective roles of smooth muscle cell phenotypic modulation and the TCF21 disease gene as revealed by single-cell analysisRobert C Wirka, Dhananjay Wagh, David T Paik, et al.
Plos Genetics|January 10, 2020
Genomic profiling of human vascular cells identifies TWIST1 as a causal gene for common vascular diseasesSylvia T Nurnberg, Marie A Guerraty, Robert C Wirka, et al.
Pageof 28